REVISION SHOULDER ARTHROPLASTY
Aseptic Loosening | Infection | Instability | Bone Loss Management
PRIMARY INDICATIONS FOR REVISION
Critical Must-Knows
- Infection is the most common indication for revision shoulder arthroplasty (40-50% of cases)
- Glenoid bone loss requires classification (Sirveaux E0-E4) and often augmentation or bone grafting
- Reverse shoulder arthroplasty is the preferred option for most revisions due to bone loss and rotator cuff deficiency
- Two-stage revision is mandatory for confirmed infection with 6-week antibiotic spacer interval
- Australian registry data (AOANJRR) shows reverse shoulder has better survivorship in revision setting
Examiner's Pearls
- "Failed hemiarthroplasty with intact rotator cuff can be converted to anatomic TSA
- "Sirveaux E3-E4 glenoid bone loss requires augmented baseplate or bone grafting
- "Humeral bone loss managed with longer stems, impaction grafting, or structural allografts
- "Subscapularis failure predisposes to instability - consider lesser tuberosity osteotomy for repair
Critical Revision Shoulder Arthroplasty Exam Points
Know Your Indications
Infection first. Always exclude infection with aspiration, CRP, ESR before revision. Two-stage mandatory if infected.
Bone Loss Classification
Sirveaux classification for glenoid (E0-E4). E3-E4 needs augmentation. Humeral side uses Morrey bone stock grading.
RSA vs Anatomic Decision
Default to RSA for most revisions. Only convert to anatomic TSA if intact rotator cuff and adequate bone stock. RSA more forgiving.
Approach and Exposure
Subscapularis management critical. Lesser tuberosity osteotomy if previous repair failed. Extended deltopectoral with careful neurovascular protection.
Quick Decision Guide: Revision Shoulder Arthroplasty
| Failed Implant | Key Features | Revision Strategy | Key Pearl |
|---|---|---|---|
| Failed hemiarthroplasty | Intact rotator cuff, good bone stock, no infection | Convert to anatomic TSA | Glenoid bone must be adequate - check for medialization |
| Failed anatomic TSA | Aseptic loosening, glenoid erosion, cuff intact | Revise to RSA or anatomic depending on bone/cuff | Assess glenoid bone loss with CT - Sirveaux grade |
| Failed RSA | Aseptic loosening, instability, or fracture | Revise to RSA with longer stem and augments | Manage bone loss - allograft, augmented baseplate, BIO-RSA |
| Any failed implant with infection | Positive aspiration, elevated inflammatory markers | Two-stage revision with antibiotic spacer | Minimum 6 weeks antibiotics, normalize CRP before reimplantation |
FAILSIndications for Revision Shoulder Arthroplasty
Memory Hook:The shoulder arthroplasty FAILS when these complications occur - each requires careful preoperative planning and often conversion to reverse!
ERODESirveaux Glenoid Bone Loss Classification
Memory Hook:Glenoid bone ERODES progressively from E0 to E4 - E3 and E4 need augmentation or grafting at revision!
IMAGESPreoperative Workup for Revision Shoulder
Memory Hook:Get complete IMAGES before revision surgery - infection exclusion and bone stock assessment are non-negotiable!
REPAIRSurgical Steps for Revision RSA
Memory Hook:REPAIR the failed shoulder - systematic component removal, bone augmentation, and soft tissue reconstruction are key!
Overview and Epidemiology
Clinical Significance of Revision Shoulder Surgery
Revision shoulder arthroplasty represents a challenging surgical problem with increasing incidence as primary shoulder replacement utilization grows. The Australian Orthopaedic Association National Joint Replacement Registry (AOANJRR) reports revision rates of 10-15% at 10 years for total shoulder arthroplasty and 8-12% for reverse shoulder arthroplasty. Infection is the most common indication (40-50%), followed by aseptic loosening (20-30%), instability (15-20%), and periprosthetic fracture (10-15%). Reverse shoulder arthroplasty has emerged as the preferred revision option due to its ability to compensate for rotator cuff deficiency and accommodate bone loss.
Demographics
- Age: Mean 65-75 years at revision (older than primary)
- Gender: Female predominance (60-65%) mirrors primary arthroplasty
- Time to revision: Mean 5-8 years from index procedure
- Multiple revisions: 10-15% require re-revision within 5 years
Clinical Impact
- Worse outcomes: Compared to primary arthroplasty (lower function, higher complications)
- Bone loss progression: Glenoid bone loss worsens with each revision
- Higher cost: 2-3 times cost of primary procedure
- Infection risk: 5-10% infection rate in aseptic revisions, up to 20% in septic
Anatomy and Biomechanical Considerations
Neurovascular Anatomy in Revision Setting
The revision shoulder arthroplasty field presents increased risk to neurovascular structures due to scar tissue, altered anatomy, and bone loss. The axillary nerve is at particular risk during inferior capsular release and glenoid exposure (average 5-7mm from inferior glenoid rim). The musculocutaneous nerve enters the coracobrachialis 5-8cm distal to the coracoid and can be injured with vigorous inferior retraction. Cephalic vein is often scarred to deltopectoral interval - careful dissection prevents avulsion and hematoma. The brachial plexus is at risk with superior-medial glenoid exposure for bone grafting.
| Structure | Location/Relevance | Risk During Revision | Protection Strategy |
|---|---|---|---|
| Axillary nerve | Exits quadrilateral space, 5-7mm from inferior glenoid | Capsular release, inferior retraction | Blunt dissection, limit inferior retraction, palpate nerve |
| Musculocutaneous nerve | Enters coracobrachialis 5-8cm from coracoid | Excessive inferior/medial retraction | Place retractors carefully, avoid prolonged tension |
| Cephalic vein | Runs in deltopectoral interval | Scar tissue can cause avulsion | Identify early, ligate if necessary, control bleeding |
| Brachial plexus | Medial to glenoid, superior to subscapularis | Medial glenoid exposure for bone grafting | Subperiosteal dissection, avoid medial drilling |
Biomechanics of Revision Shoulder Arthroplasty
Glenoid Bone Loss Biomechanics
- Medialization: Each 1mm medial shift reduces deltoid lever arm by 2-3%
- Retroversion: Increased retroversion causes posterior subluxation and eccentric loading
- Superior tilt: Superior tilt greater than 10 degrees increases shear forces and failure risk
- Baseplate fixation: Minimum 4 screws required for stable fixation in revision setting
Humeral Bone Loss Biomechanics
- Stem stability: Longer stems required for fixation past bone loss zone (150-200mm)
- Cement use: Cemented stems recommended for poor bone quality or cortical thinning
- Impaction grafting: Restores bone stock for potential future revision
- Stress shielding: Minimize with modular stems and anatomic reaming
Classification Systems
Sirveaux Classification (Glenoid Bone Loss in Failed RSA)
| Grade | Description | Bone Loss | Management |
|---|---|---|---|
| E0 | No bone loss - intact glenoid surface | 0% | Standard glenoid baseplate, no augmentation |
| E1 | Round erosion - central defect less than 50% width | Under 25% | Standard baseplate with central screw or BIO-RSA |
| E2 | Oblique erosion - eccentric biconcave pattern | 25-40% | Eccentric reaming or small augmented baseplate |
| E3 | Deep central erosion greater than 50% width | 40-60% | Augmented baseplate or structural bone graft required |
| E4 | Extensive superior and medial bone loss | Over 60% | Structural allograft, BIO-RSA, or custom implants |
Sirveaux E3 vs E4 Distinction
E3 has deep central erosion but intact superior and medial glenoid cortex - can be managed with augmented baseplate or bone graft impaction. E4 has extensive superior and medial bone loss with loss of structural integrity - requires structural allograft (scapular spine bone graft, iliac crest strut graft) or BIO-RSA (bony-increased offset RSA with large bone graft). The distinction is critical because E4 has significantly higher failure rates without structural grafting.
Clinical Assessment
History
- Onset of symptoms: Acute vs gradual onset (infection vs aseptic loosening)
- Pain character: Rest pain suggests loosening/infection; activity pain suggests instability
- Prior surgeries: Number of revisions, previous infections, complications
- Functional loss: What patient can no longer do (overhead activities, lifting)
- Systemic symptoms: Fevers, night sweats, weight loss (infection red flags)
- Current antibiotics: Recent antibiotic use may mask infection
Examination
- Look: Scars, drainage, erythema, muscle atrophy (deltoid, supraspinatus)
- Feel: Warmth, effusion, component prominence, crepitus
- Move: Active and passive ROM - distinguish true ROM from scapulothoracic compensation
- Strength: Deltoid, rotator cuff testing (external rotation, belly press for subscapularis)
- Stability: Anterior/posterior load-shift test, sulcus sign for inferior laxity
- Neurovascular: Axillary nerve (deltoid), musculocutaneous (biceps), radial pulse
Beware the Infected Revision
Infection can present insidiously in revision shoulder arthroplasty. Red flags include: progressive pain without mechanical symptoms, persistent drainage beyond 3 weeks postoperatively, elevated inflammatory markers (CRP greater than 10 mg/L, ESR greater than 30 mm/hr after 3 months), persistent shoulder effusion, or radiographic signs (periosteal reaction, progressive osteolysis). Low-grade infections with Cutibacterium acnes may present with only pain and stiffness without systemic symptoms. Always aspirate suspicious shoulders before revision surgery - cultures must be held for 14 days for Cutibacterium detection.
Differential Diagnosis
| Diagnosis | Clinical Features | Key Investigations | Treatment |
|---|---|---|---|
| Aseptic loosening | Gradual onset pain, mechanical symptoms, normal inflammatory markers | Serial radiographs showing progressive radiolucency | Revision to RSA in most cases |
| Infection | Pain, stiffness, elevated CRP/ESR, possible drainage | Aspiration with extended 14-day cultures, CRP greater than 10 | Two-stage revision with spacer |
| Instability | Clunking, apprehension, recurrent dislocation | CT showing component malposition or glenoid bone loss | Revision to RSA with increased offset |
| Periprosthetic fracture | Acute onset pain and loss of function after fall or minor trauma | Radiographs or CT showing fracture around components | Revision with fracture fixation if unstable |
Investigations
Imaging and Laboratory Protocol
Views required: True AP (Grashey), axillary lateral, scapular Y. What to look for:
- Component position (version, height, tilt)
- Radiolucency greater than 2mm (glenoid or humeral loosening)
- Periprosthetic fracture
- Heterotopic ossification
- Baseplate screw breakage or hardware migration
- Glenoid notching (Sirveaux grades in RSA)
- Humeral stem subsidence or loosening lines
Key measurements: Glenoid version (normal 5 degrees retroversion), superior tilt (less than 10 degrees acceptable), humeral offset.
Gold standard for bone stock assessment. Obtain 3D reconstructions. Critical information:
- Quantify glenoid bone loss (Sirveaux classification)
- Glenoid version, inclination, medialization
- Humeral bone stock and canal dimensions
- Baseplate fixation and screw trajectories
- Plan bone graft needs and augmented implants
- Identify occult fractures
Sensitivity: 95% for glenoid loosening detection, 90% for bone loss quantification.
Mandatory infection screening before revision:
- CRP: Greater than 10 mg/L after 3 months suggests infection (sensitivity 85%)
- ESR: Greater than 30 mm/hr after 3 months (sensitivity 70%, less specific than CRP)
- Shoulder aspiration: Pre-operative aspiration off antibiotics for 2 weeks
- Extended cultures: Hold for 14 days minimum for Cutibacterium acnes detection
- Synovial fluid analysis: WBC greater than 3000, PMN greater than 70% suggests infection
- Frozen section: Greater than 5 PMN per high-power field (intraoperative confirmation)
Pearl: Standard 5-day cultures miss 20-30% of shoulder infections. Extended 14-day cultures are non-negotiable.
Indications for MRI:
- Assess rotator cuff status if considering conversion to anatomic TSA
- Evaluate soft tissue masses (infection, tumor)
- Assess subscapularis integrity for surgical planning
- Metal artifact reduction sequences (MARS) protocols for better visualization
Limitations: Metal artifact from prosthesis limits resolution. CT usually more helpful for bone assessment.
Imaging Gallery
Management Algorithm
Aseptic Revision Shoulder Arthroplasty Algorithm
Goal: Restore shoulder function with durable fixation despite bone loss and soft tissue compromise.
Decision Making and Surgical Steps
- CRP, ESR, shoulder aspiration with 14-day extended cultures
- Hold antibiotics for 2 weeks before aspiration
- If positive cultures or high clinical suspicion → proceed to two-stage revision
- If negative → proceed with aseptic revision planning
- CT scan with 3D reconstruction (mandatory for revision planning)
- Classify glenoid bone loss: Sirveaux E0-E4
- Assess humeral bone stock: Morrey classification
- Plan for augmented baseplate (E3-E4) or bone grafting
- Determine stem length for humeral revision
Failed Hemiarthroplasty:
- If intact rotator cuff and good glenoid bone → convert to anatomic TSA
- If cuff deficiency or moderate bone loss → convert to RSA
Failed Anatomic TSA:
- Default to RSA for most cases (more forgiving of bone loss and cuff issues)
- Consider anatomic revision only if intact cuff, minimal bone loss, and young active patient
Failed RSA:
- Revise to RSA with longer stem, augmented baseplate, or bone grafting
- Manage instability with increased lateralization and offset
- Extended deltopectoral approach with subscapularis management
- Careful component extraction minimizing bone loss
- Address bone defects with augmented implants or structural grafting
- Secure baseplate fixation (minimum 4 screws)
- Subscapularis repair or lesser tuberosity osteotomy
RSA vs Anatomic TSA Decision in Revision
Default to reverse shoulder arthroplasty for most revision cases. RSA compensates for rotator cuff deficiency (common after failed TSA), accommodates glenoid bone loss better than anatomic TSA (medialization is less detrimental), and has better survivorship in the revision setting per AOANJRR data. Only convert failed hemiarthroplasty to anatomic TSA if: (1) intact rotator cuff confirmed on MRI or intraoperatively, (2) adequate glenoid bone stock (E0-E1 Sirveaux), (3) no component malposition requiring excessive bone removal. If in doubt, choose RSA.
Surgical Technique
Preoperative Planning and Consent
Consent Points
- Infection: 5-10% risk in aseptic revision, up to 20% if septic two-stage
- Nerve injury: 5% risk (axillary nerve most common)
- Instability: 10-15% recurrent dislocation risk
- Need for bone grafting: May need iliac crest or allograft if severe bone loss
- Need for re-revision: 10-15% require further surgery within 5 years
- Stiffness/pain: 20% have persistent pain despite revision
- Medical risks: DVT/PE (1-2%), anesthesia complications
Equipment Checklist
- Implants: Revision RSA system with augmented baseplates, long humeral stems (150-200mm), bone graft options
- Power tools: High-speed burr, reciprocating saw, flexible osteotomes
- Component extraction tools: Explantation instruments, thin flexible osteotomes, gigli saw
- Imaging: C-arm positioned for AP and axillary views
- Bone graft: Iliac crest instruments on standby, allograft femoral head available
- Cultures: Culture bottles and specimen containers for tissue samples
Implant Planning - Have Backup Options
Revision shoulder arthroplasty often encounters unexpected intraoperative findings. Always have available: (1) multiple glenoid baseplate sizes and augmented options, (2) range of humeral stem lengths (standard, long, extra-long), (3) structural allograft (femoral head, distal femur), (4) bone graft substitutes (cancellous chips, demineralized bone matrix), (5) antibiotic-laden cement for humeral fixation. Confirm all implants are in the OR before incision - intraoperative delays for missing components increase infection risk and operative time.
Complications
| Complication | Incidence | Risk Factors | Management |
|---|---|---|---|
| Infection | 5-10% in aseptic revision, 10-20% in septic two-stage | Previous infection, multiple revisions, immunosuppression, diabetes | Two-stage revision with antibiotic spacer, 6 weeks IV antibiotics |
| Instability | 10-15% recurrent dislocation | Subscapularis failure, component malposition, inadequate soft tissue tension | Revise to RSA with increased offset, thicker polyethylene, subscapularis repair |
| Aseptic loosening | 5-10% at 5 years | Poor bone stock, inadequate fixation, infection | Re-revision with bone grafting, augmented baseplate, or structural allograft |
| Periprosthetic fracture | 3-5% intraoperative, 2-3% postoperative | Osteoporosis, aggressive component extraction, cortical perforation | Intraop: cerclage wiring, longer stem. Postop: ORIF vs revision depending on fracture pattern and implant stability |
| Nerve injury | 3-5% (axillary most common) | Excessive retraction, prolonged operative time, traction injury | Observation (most recover spontaneously), EMG at 3 months, nerve exploration if no recovery at 6 months |
| Stiffness | 15-20% significant ROM limitation | Overtensioned soft tissues, capsular scarring, heterotopic ossification | Intensive PT, consider manipulation under anesthesia if severe and early (within 3 months) |
| Scapular notching | 20-30% in RSA | Inferior glenosphere position, small glenosphere size, medialized center of rotation | Usually asymptomatic. If symptomatic loosening, revise with lateralized glenosphere |
Early Recognition of Deep Infection
Early infection (within 4 weeks) may be salvageable with DAIR (debridement, antibiotics, and implant retention) if recognized immediately. Red flags: persistent drainage beyond 72 hours, fever, purulent drainage, elevated WBC. Protocol: (1) Return to OR immediately (within 24-48 hours of symptom onset). (2) Aggressive debridement and synovectomy. (3) Polyethylene exchange. (4) Obtain cultures before antibiotics. (5) 6 weeks IV antibiotics based on cultures. Success rate: 40-60% for acute infections caught early. Delayed recognition (beyond 4 weeks) requires two-stage revision - DAIR will fail in chronic infections (success rate under 20%).
Complication Prevention Strategies
Infection Prevention
- Preoperative optimization: Control diabetes (HbA1c under 7%), discontinue immunosuppression if possible
- Antibiotic prophylaxis: Cefazolin 2g (3g if over 120kg) within 1 hour of incision
- Extended prophylaxis: Continue 24 hours postoperatively for revision cases
- Operative time: Minimize time (longer surgeries = higher infection risk)
- Meticulous hemostasis: Hematoma is infection risk
- Wound closure: Multiple layer closure, avoid tension
Instability Prevention
- Component positioning: Correct glenoid version (0-10 degrees retroversion), avoid excessive humeral retroversion
- Soft tissue balancing: Adequate polyethylene thickness, subscapularis repair
- Intraoperative stability testing: Test through full ROM before closure
- Lateralization: Consider lateralized glenosphere for increased stability (36mm or 42mm vs 32mm)
- Postoperative protection: Abduction sling for 6 weeks protects subscapularis
Postoperative Care and Rehabilitation
Rehabilitation Timeline
Hospital management:
- Abduction sling with pillow (30 degrees abduction)
- Drain management if placed (remove when output under 30mL per 8 hours)
- Pain control: Regional block (interscalene catheter for 2-3 days), oral narcotics
- DVT prophylaxis: Mechanical (sequential compression devices), chemical (enoxaparin 40mg daily) if low bleeding risk
- Antibiotics: Continue prophylaxis for 24 hours (cefazolin 1g every 8 hours)
- Early mobilization: Out of bed to chair on postoperative day 0-1
Discharge: Usually postoperative day 1-2 for uncomplicated cases.
Protection phase:
- Abduction sling full-time (remove for exercises and hygiene only)
- No active internal rotation (protects subscapularis repair)
- Passive ROM only: Therapist-assisted forward elevation to 120 degrees, abduction to 90 degrees, external rotation to 30 degrees
- Pendulum exercises 3 times daily
- Grip strengthening
- Elbow, wrist, hand ROM to prevent stiffness
Goals: Protect subscapularis while preventing stiffness. ROM goals at 6 weeks: Forward elevation 120 degrees passive, external rotation 30 degrees.
Follow-up: Week 2 (wound check, remove staples), Week 6 (radiographs to assess healing, progress PT).
Active motion phase:
- Wean from abduction sling at 6 weeks if radiographs satisfactory and clinical exam reassuring
- Progress to active-assisted ROM (pulley exercises, cane-assisted elevation)
- Begin active ROM at week 8 (deltoid-driven forward elevation and abduction)
- Light internal rotation at week 8-10 (hand to belly, hand to opposite shoulder)
- Continue to avoid forceful internal rotation (subscapularis still healing)
Goals: Active forward elevation to 140 degrees, active abduction to 100 degrees, external rotation to 45 degrees by week 12.
Follow-up: Week 12 radiographs and clinical assessment.
Progressive strengthening:
- Resistance band exercises for deltoid, rotator cuff (avoid heavy internal rotation)
- Scapular stabilization exercises (rows, scapular squeezes)
- Functional activities (reaching, lifting light objects)
- Gradual return to activities of daily living
- Continue home exercise program indefinitely
Goals: Functional ROM and strength for daily activities. Forward elevation 150-160 degrees, abduction 120-140 degrees, functional internal rotation.
Follow-up: 6 months, 1 year, then yearly radiographs to monitor for loosening or complications.
Annual follow-up:
- Clinical assessment: Pain, function, ROM, strength
- Radiographs: AP and axillary views to assess component position, lucencies, scapular notching
- Monitor for late complications: Infection, loosening, instability, scapular notching progression
Patient education:
- Avoid heavy overhead lifting (over 10kg)
- No contact sports or high-impact activities
- Report new pain, clicking, or instability immediately
- Maintain shoulder ROM with home exercises
The Critical 6-Week Window
The first 6 weeks are critical for subscapularis healing and determine long-term stability. Patients must understand: (1) No active internal rotation means no reaching behind back, no pulling shirt on, no forceful activities. (2) Sling compliance is non-negotiable - remove only for exercises and hygiene. (3) Passive motion is safe and necessary - stiffness is preventable but subscapularis failure is catastrophic. (4) At 6-week visit, assess subscapularis integrity with belly press test - if strong, progress to active motion; if weak, continue protection and repeat at 8 weeks. (5) Early return to internal rotation (before 6 weeks) results in 60-80% subscapularis failure rate with permanent anterior instability.
Outcomes and Prognosis
| Revision Type | Survivorship at 5 Years | Typical Outcomes | Notes |
|---|---|---|---|
| Aseptic revision to RSA | 85-90% | Good pain relief, functional ROM (140 degrees FE average), return to light ADLs | Outcomes inferior to primary RSA but acceptable for most patients |
| Aseptic revision to anatomic TSA | 75-85% | Good outcomes if intact cuff and good bone stock, but higher revision rate than RSA | Only recommended for select cases with excellent bone and cuff |
| Two-stage septic revision | 70-80% | Infection eradication 85-90%, but 15-20% reinfection. Function similar to aseptic if successful | Reinfection requires prolonged antibiotics or resection arthroplasty |
| Revision for instability | 70-75% | 50-60% achieve stable shoulder, but 15-20% recurrent instability despite revision | Multiple revisions for instability have poor outcomes |
| Re-revision (3rd surgery) | 60-70% | Diminishing returns with each revision. Consider resection arthroplasty if multiple failures | Patient selection critical - counsel realistic expectations |
Predictors of Poor Outcome After Revision
Poor prognostic factors for revision shoulder arthroplasty: (1) Multiple prior revisions (each revision decreases success rate by 15-20%). (2) Severe glenoid bone loss (Sirveaux E4 has 2-3 times higher failure rate than E0-E2). (3) Infection as indication (septic revisions have 15-20% reinfection rate vs 5-10% infection rate in aseptic revisions). (4) Neurological injury (axillary nerve injury results in poor functional outcomes despite stable implant). (5) Poor soft tissue envelope (deltoid insufficiency, subscapularis irreparable). (6) Patient factors (diabetes, smoking, immunosuppression, age over 80). Best outcomes: Single aseptic revision to RSA with intact soft tissues and moderate bone loss (E1-E2).
Functional Outcomes
ROM Expectations
Typical ROM after revision RSA:
- Forward elevation: 120-140 degrees (vs 150-160 for primary)
- Abduction: 100-120 degrees (vs 130-150 for primary)
- External rotation: 30-40 degrees (vs 40-50 for primary)
- Internal rotation: Limited (hand to belly vs hand to low back for primary)
Functional impact: Most patients can perform overhead ADLs (eating, hygiene, dressing) but limited for heavy lifting or overhead work.
Pain Relief and Satisfaction
- Pain relief: 80-85% achieve significant pain improvement (VAS 7-8 to VAS 2-3)
- Patient satisfaction: 70-75% satisfied or very satisfied (vs 85-90% for primary)
- Return to activities: 60-70% return to light recreational activities (golf, swimming)
- Work: 50-60% able to return to work if pre-retirement age
Realistic expectations: Patients must understand revision outcomes are inferior to primary arthroplasty.
Evidence Base and Key Trials
Reverse Shoulder Arthroplasty for Failed Shoulder Arthroplasty
- Retrospective series of 45 failed shoulder arthroplasties revised to RSA
- 78% good or excellent outcomes at mean 40-month follow-up
- Significant improvement in Constant score from 22 to 54 points
- 15% complication rate including infection (7%) and instability (4%)
- Glenoid bone loss (Sirveaux E3-E4) associated with higher revision rates
Two-Stage Revision for Infected Shoulder Arthroplasty
- Systematic review of 175 infected shoulder arthroplasties treated with two-stage revision
- Infection eradication rate 84% (147/175 patients)
- Cutibacterium acnes most common organism (38% of cases)
- Mean antibiotic interval 12 weeks (range 4-24 weeks)
- Functional outcomes inferior to aseptic revisions but acceptable pain relief
Glenoid Bone Loss Management in Revision RSA
- Biomechanical study and clinical series of 34 revision RSA cases with severe glenoid bone loss
- Augmented baseplates restored glenoid version and stability in E3 defects
- Structural bone grafting required for E4 defects (over 60% bone loss)
- Baseplate failure rate 12% at 3-year follow-up (higher in E4 vs E3)
- Medialization greater than 5mm associated with decreased deltoid efficiency and outcomes
Australian Orthopaedic Association National Joint Replacement Registry (AOANJRR)
- 10-year cumulative revision rate for primary shoulder arthroplasty: 10.2% for TSA, 8.4% for RSA
- Revision shoulder arthroplasty has 2.5 times higher re-revision rate than primary (25% vs 10% at 10 years)
- Infection is most common indication for revision (48% of revisions)
- RSA used in 72% of revision procedures (vs 28% anatomic TSA)
- Cemented humeral stems have lower revision rates than uncemented in revision setting (7% vs 12% at 5 years)
Functional Outcomes After Revision Shoulder Arthroplasty: Systematic Review
- Systematic review of 23 studies including 892 revision shoulder arthroplasties
- Mean Constant score improvement from 28 to 56 points post-revision
- Mean forward elevation 132 degrees post-revision (vs 150 degrees for primary RSA)
- Complication rate 18% (infection 6%, instability 5%, nerve injury 3%, fracture 4%)
- Revision to RSA had better outcomes than revision to anatomic TSA (Constant score 58 vs 48)
Exam Viva Scenarios
Practice these scenarios to excel in your viva examination
Scenario 1: Failed Hemiarthroplasty (~3 min)
"A 62-year-old woman presents with progressive shoulder pain 5 years after hemiarthroplasty for fracture sequelae. She has painful limited ROM. Radiographs show glenoid erosion with medialization. CRP 5 mg/L, ESR 15 mm/hr. Aspiration shows no growth on 5-day cultures. What is your assessment and management?"
Scenario 2: Failed Reverse Shoulder with Instability (~4 min)
"A 68-year-old man had reverse shoulder arthroplasty 2 years ago for cuff tear arthropathy. He now has recurrent anterior dislocations (3 episodes in 6 months). Radiographs show well-fixed components with 32mm glenosphere, standard polyethylene insert, and neutral glenoid version. Belly press test is weak. Walk me through your revision planning and surgical technique."
Scenario 3: Infected Shoulder Arthroplasty (~3 min)
"A 71-year-old diabetic woman presents 8 months after reverse shoulder arthroplasty with persistent pain, no improvement in function, and occasional drainage from the incision. CRP 25 mg/L, ESR 45 mm/hr. Aspiration grows Staphylococcus epidermidis (2 of 3 bottles). She is devastated and asks if you can just give antibiotics. How do you manage this case and what is your counseling?"
MCQ Practice Points
Glenoid Bone Loss Question
Q: What is the Sirveaux classification for glenoid bone loss in failed reverse shoulder arthroplasty, and what is the threshold for requiring augmented baseplate or bone grafting? A: The Sirveaux classification grades glenoid bone loss from E0 (no loss) to E4 (extensive superior and medial loss). E0-E2 can be managed with standard glenoid baseplate or eccentric reaming. E3 (deep central erosion greater than 50% width) and E4 (extensive bone loss) require augmented baseplate or structural bone grafting. E3 can often be managed with augmented baseplate alone, while E4 typically requires structural allograft (scapular spine bone graft or BIO-RSA technique).
Infection Workup Question
Q: Why are extended 14-day cultures required for suspected shoulder prosthetic joint infection, and what is the most common organism? A: Cutibacterium acnes (formerly Propionibacterium) is the most common organism in shoulder prosthetic joint infection (30-40% of cases) and is a slow-growing anaerobe requiring 14 days of culture incubation for detection. Standard 5-day cultures miss 20-30% of shoulder infections. Cutibacterium is low-virulence and can cause indolent infection with minimal systemic symptoms, making extended cultures essential even when clinical suspicion is low.
RSA vs Anatomic TSA Decision Question
Q: What factors favor conversion to reverse shoulder arthroplasty vs anatomic total shoulder arthroplasty when revising a failed hemiarthroplasty? A: Favor reverse shoulder arthroplasty (most common choice): (1) Rotator cuff deficiency or massive cuff tear, (2) Moderate to severe glenoid bone loss (Sirveaux E2-E4), (3) Patient age over 70 years, (4) Low functional demands, (5) Deltoid function intact. Favor anatomic TSA (uncommon): (1) Intact rotator cuff confirmed on MRI or intraoperatively, (2) Minimal glenoid bone loss (E0-E1), (3) Younger patient (under 60 years), (4) High functional demands, (5) Adequate glenoid bone stock after component removal. Default to RSA if uncertain - more forgiving of bone loss and cuff deficiency.
Two-Stage Revision Protocol Question
Q: What are the key steps and success rates for two-stage revision of infected shoulder arthroplasty? A: Two-stage revision protocol: (1) Stage 1 - Complete removal of all components and cement, synovectomy, debridement of infected tissue, minimum 5 tissue cultures (14-day hold), antibiotic-impregnated cement spacer (vancomycin 4g and tobramycin 2.4g per 40g cement), followed by 6 weeks IV antibiotics. (2) Antibiotic holiday - Hold antibiotics for minimum 2 weeks, repeat CRP and ESR (goal: CRP less than 10 mg/L, ESR less than 30 mm/hr). (3) Stage 2 - Reimplantation if inflammatory markers normalized, obtain fresh tissue cultures and frozen section (less than 5 PMN per HPF required to proceed), followed by 3-6 months oral suppressive antibiotics. Success rate: 85-90% infection eradication, but 10-15% reinfection risk. Functional outcomes similar to aseptic revision if infection cleared.
Subscapularis Management Question
Q: What are the options for subscapularis management in revision shoulder arthroplasty, and which has the best healing rate? A: Subscapularis options: (1) Direct tendon repair - If subscapularis intact and good tissue quality, repair with transosseous sutures or suture anchors (success rate 50-60% in revision). (2) Lesser tuberosity osteotomy - If poor tissue quality or previous repair failed, perform 10-15mm thick osteotomy with two screw fixation (success rate 80-90% with bone-to-bone healing). (3) Accept insufficiency - If subscapularis irreparable, proceed without repair and compensate with increased component constraint or glenosphere lateralization (higher anterior instability risk). Lesser tuberosity osteotomy is preferred in revision setting due to superior healing and allows bone-to-bone contact. Protection for 6 weeks with no active internal rotation is mandatory for either repair technique.
AOANJRR Registry Data Question
Q: What does the Australian Orthopaedic Association National Joint Replacement Registry (AOANJRR) report regarding revision shoulder arthroplasty indications and implant choice? A: AOANJRR 2023 data: (1) Most common indication for revision is infection (48% of all revisions), followed by aseptic loosening (28%) and instability (15%). (2) Reverse shoulder arthroplasty is used in 72% of revision procedures vs 28% anatomic TSA. (3) Cemented humeral stems have lower re-revision rates than uncemented in the revision setting (7% vs 12% at 5 years). (4) Cumulative re-revision rate at 10 years is 25% for revision shoulders vs 10% for primary arthroplasty (2.5 times higher). This data supports RSA as the preferred revision option and cemented humeral fixation for improved survivorship.
Australian Context and Medicolegal Considerations
AOANJRR Data and Guidelines
- Revision rates: 10-year cumulative revision 10.2% for TSA, 8.4% for RSA (2023 report)
- Infection dominance: 48% of revisions due to infection (higher than hip or knee)
- RSA preference: 72% of revisions use RSA (reflects bone loss and cuff deficiency)
- Cemented stems: Cemented humeral fixation associated with lower re-revision rates in revision setting
- Hospital volume: Higher volume centers (over 50 shoulder arthroplasties per year) have lower revision rates
- Annual reporting: Registry participation mandatory for all arthroplasty cases in Australia
Australian Clinical Guidelines
- ACSQHC Surgical Site Infection Prevention: Preoperative skin preparation with chlorhexidine-alcohol, appropriate antibiotic prophylaxis (cefazolin 2g within 60 minutes)
- Antimicrobial Stewardship: Extended antibiotic prophylaxis (24 hours) acceptable for revision cases per Therapeutic Guidelines (eTG)
- VTE Prophylaxis: NHMRC guidelines recommend mechanical prophylaxis for all cases, chemical prophylaxis (enoxaparin) for high-risk patients
- Perioperative Diabetes Management: Target HbA1c under 7% for elective arthroplasty per ANZCA guidelines
- PBS Restrictions: Some revision implants require prior approval for PBS subsidy
Medicolegal Considerations in Revision Shoulder Arthroplasty
Key documentation requirements for revision cases:
Preoperative Counseling (document in medical record):
- Realistic outcome expectations (outcomes inferior to primary by 30-40%)
- Infection risk specific to revision setting (5-10% aseptic, 10-20% septic two-stage)
- Need for bone grafting if severe bone loss discovered intraoperatively
- Possibility of re-revision (10-15% at 5 years)
- Alternative treatment options (non-operative management, arthrodesis, resection arthroplasty)
- Two-stage process for infected cases with prolonged treatment timeline
Intraoperative Documentation:
- Indication for revision (aseptic loosening, infection, instability, fracture)
- Infection workup results (cultures, inflammatory markers, aspiration)
- Bone stock assessment and classification (Sirveaux grade for glenoid)
- Implant choices and rationale (RSA vs anatomic TSA, augmented components, bone grafting)
- Tissue samples sent for culture and pathology
- Subscapularis management technique
- Complications encountered (fracture, nerve injury, bleeding)
Postoperative Care:
- Clear rehabilitation protocol with subscapularis protection guidelines
- Antibiotic regimen for infection cases with infectious disease consultation
- Follow-up plan with inflammatory marker monitoring
- Radiographic surveillance for loosening or complications
Common Litigation Issues:
- Failure to exclude infection before aseptic revision (results in persistent infection)
- Inadequate bone stock assessment leading to early failure
- Subscapularis repair failure from inadequate protection or technique
- Nerve injury from excessive retraction or direct trauma
- Inadequate informed consent regarding realistic outcomes
Risk Management: Document detailed preoperative discussion, obtain infectious disease consultation for septic cases, ensure adequate radiographic assessment (CT for bone stock), clear postoperative instructions, and close follow-up with inflammatory marker monitoring.
Australian Hospital Protocols
Public Hospital Pathways
- Outpatient Services: Elective revision shoulder referred through outpatient clinics with 6-12 month wait times (Category 2-3)
- Infection cases: Fast-tracked as Category 1 (within 30 days) if symptomatic infection
- MDT approach: Complex revisions discussed at multidisciplinary meeting (orthopedics, infectious disease, radiology)
- Resource allocation: Revision cases require specialized implants and longer operative time (2-4 hours) - pre-approve with hospital
- Allied health: Physiotherapy review prior to discharge, outpatient PT for 3-6 months postop
Private Hospital Considerations
- Insurance coverage: Check private health insurance excess and coverage for revision implants (can be 2-3 times cost of primary)
- Gap payments: Inform patients of potential out-of-pocket costs for revision surgery
- Prosthesis funding: Some revision implants not fully covered by prosthesis list - discuss with patient
- Hospital choice: Ensure hospital has revision implant inventory and expertise
- Medico-legal: Private practitioners require comprehensive informed consent and documentation
REVISION SHOULDER ARTHROPLASTY
High-Yield Exam Summary
Key Indications
- •Infection = most common indication (40-50% of revisions) - requires two-stage with 6-week antibiotics
- •Aseptic loosening = 20-30% - progressive pain and radiolucency, revise to RSA
- •Instability = 15-20% - subscapularis failure or malposition, increase offset and repair
- •Periprosthetic fracture = 10-15% - revise if unstable, ORIF if stable implant
Glenoid Bone Loss Classification
- •Sirveaux E0 = no bone loss - standard baseplate
- •Sirveaux E1 = round erosion under 50% - standard or BIO-RSA
- •Sirveaux E2 = oblique erosion - eccentric reaming or small augment
- •Sirveaux E3 = deep central erosion over 50% - augmented baseplate required
- •Sirveaux E4 = extensive superior/medial loss - structural bone graft + BIO-RSA
Surgical Pearls
- •Extended 14-day cultures mandatory for Cutibacterium acnes (30-40% of infections)
- •Default to RSA for most revisions - more forgiving of bone loss and cuff deficiency
- •Lesser tuberosity osteotomy for failed subscapularis (80-90% healing vs 50-60% for tendon repair)
- •Cemented humeral stems preferred in revision (better fixation in compromised bone)
- •Minimum 4 screws for glenoid baseplate fixation (preferably 6 for revision)
- •Bypass bone loss by 2 cortical diameters with humeral stem (8-10cm minimum)
Two-Stage Infection Protocol
- •Stage 1 = explantation, debridement, antibiotic spacer (vancomycin 4g + tobramycin 2.4g per 40g cement)
- •6 weeks IV antibiotics based on cultures, then 2-week antibiotic holiday
- •Stage 2 = reimplant if CRP less than 10 mg/L and ESR less than 30 mm/hr off antibiotics
- •Frozen section less than 5 PMN per HPF required to proceed with reimplantation
- •85-90% infection eradication rate, 10-15% reinfection risk despite protocol
Complications
- •Infection = 5-10% in aseptic revision, 10-20% in septic two-stage
- •Instability = 10-15% recurrent dislocation - manage with larger glenosphere, thicker poly, subscap repair
- •Re-revision = 10-15% at 5 years (2.5x higher than primary per AOANJRR)
- •Nerve injury = 3-5% (axillary most common) - observation, most recover spontaneously
- •Periprosthetic fracture = 3-5% intraop - cerclage wiring and longer stem
Key Evidence and Registry Data
- •AOANJRR 2023: Infection accounts for 48% of revisions, RSA used in 72% of revision cases
- •Boileau 2009: RSA for failed arthroplasty achieves 78% good/excellent outcomes at 40 months
- •Klatte 2013: Two-stage revision achieves 84% infection eradication for shoulder PJI
- •Favre 2018: Augmented baseplates effective for E3 bone loss, structural grafting needed for E4
- •Chalmers 2020: Revision RSA superior to anatomic TSA (Constant 58 vs 48 points)